DrugNov 6, 2024
Chlorpheniramine Maleate 4 mg tablets, 24-count bottle recall — FDA D-0029-2025
Superpotent Drug: Stability failure for assay at 6 months test time-point.
Class IIFDA: TerminatedBLI International, Inc.
Latest records
Latest recalls — page 310
The newest recall records with useful source details are listed here.
VehicleNov 4, 2024
BMW roof and pillars recall — NHTSA campaign 24V829000
BMW of North America, LLC (BMW) is recalling certain 2025 X1 xDrive28i and X1 M35i vehicles. The left and right-side B-Pillar reinforcement plates may have been manufactured with…
roof and pillarsBMW of North America, LLC
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TranStar KIDS KIT 31IN recall — FDA Z-0198-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Boston Scientific myLUX Patient Application for an Apple Mobile device, Model Number 2939 recall — FDA Z-0226-2025
Patients using the Model 2939 myLUX Patient Application on their Apple mobile device (e.g., iPhone) may not be transmitting data from their Insertable Cardiac Monitor to the LATITUDE…
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceOct 30, 2024
Datex-Ohmeda Aespire View. This anesthesia gas machine is intended to provide general recall — FDA Z-0077-2025
Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port.
Class IFDA: OngoingDatex-Ohmeda, Inc.
Medical DeviceOct 30, 2024
Medline brand medical procedure convenience kits, labeled as: a) CONE BIOPSY PACK, REF recall — FDA Z-0158-2025
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceOct 30, 2024
MEDLINE INDUSTRIES, LP - Northfield Centurion brand, medical procedure convenience kits recall — FDA Z-0150-2025
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceOct 30, 2024
Datex-Ohmeda Auxiliary Common Gas Outlet (ACGO) conversion/install kits sold under product recall — FDA Z-0084-2025
Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port.
Class IFDA: OngoingDatex-Ohmeda, Inc.
Medical DeviceOct 30, 2024
Olympus Corporation of the Americas Soltive Pro SuperPulsed Laser Systems-Intended for recall — FDA Z-0135-2025
The term Bladder Stone was incorrectly translated in both Spanish and Portuguese to Kidney Stone(Clculo renal) on the systems Graphical User Interface (GUI), a potential to deliver an…
Class IIFDA: OngoingOlympus Corporation of the Americas
Medical DeviceOct 30, 2024
Medline CV ANESTHESIA - ROOM SET UP, REF DYNJ905503F recall — FDA Z-0152-2025
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceOct 30, 2024
Mckesson Medical-Surgical Inc. Corporate Office Quantimetrix Urine Chemistry Control Set recall — FDA Z-0138-2025
The Quantimetrix Dipper Urinalysis Dipstick control was shipped without the validated summer packaging and may have been exposed to temperatures above 25¿C. This may lead to delay in…
Class IIFDA: OngoingMckesson Medical-Surgical Inc. Corporate Office
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TranStar Disposable Transducer 1/EA, Product Code REF MX950 recall — FDA Z-0188-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TranStar KIDS KIT 19IN recall — FDA Z-0197-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Medline brand medical procedure convenience kits, labeled as: a) OB PACK-LF, REF recall — FDA Z-0177-2025
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceOct 30, 2024
Smiths Medical ASD medex NICU Monitoring Kit Set 1/EA, Product Code REF MX20086 recall — FDA Z-0184-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Medline brand medical procedure convenience kits, labeled as: a) KIT LINE INSERTION, REF recall — FDA Z-0157-2025
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceOct 30, 2024
Spectrum Medical Quantum Perfusion Systems for CPB, Roller Pumps use peristaltic action to recall — FDA Z-0224-2025
The ratchet and pawl had an out of tolerance geometry which exhibited as the left bobbin would not lock.
Class IIFDA: CompletedSpectrum Medical Ltd.
Medical DeviceOct 30, 2024
SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION Trinias unity, Digital Angiography System with recall — FDA Z-0139-2025
If digital angiography system is used with a specific catheterization table and the operator directs simultaneous movement of the table and the C-arm using direct memory, then direct memory…
Class IIFDA: OngoingSHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION
Medical DeviceOct 30, 2024
Medline PEDIATRIC DRAPE PK, REF DYNJ81297 recall — FDA Z-0169-2025
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TranStar Kit w/ Stopcock1/EA, Product Code REF MX20740 recall — FDA Z-0186-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Medline brand medical procedure convenience kits, labeled as: a) NEURO PACK, REF DYNJ37909A recall — FDA Z-0173-2025
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
Medical DeviceOct 30, 2024
Smiths Medical ASD medex TranStar Neonatal Monitoring Kit 10/EA, Product Code REF MX9530T recall — FDA Z-0196-2025
Due to a manufacturing defect, users may experience inaccurate pressure monitoring, an interruption in pressure monitoring, or an inability to zero the device due to either a leak within…
Class IIFDA: OngoingSmiths Medical ASD, Inc.
Medical DeviceOct 30, 2024
Datex-Ohmeda Aespire 7900. This anesthesia gas machine is intended to provide general recall — FDA Z-0076-2025
Potential issue that may arise if the limb of a patient breathing circuit is mistakenly connected to the Auxiliary Common Gas Outlet (ACGO) port.
Class IFDA: OngoingDatex-Ohmeda, Inc.
Medical DeviceOct 30, 2024
Medline brand medical procedure convenience kits, labeled as: 1) T&A CDS-LF, REF CDS982091I recall — FDA Z-0160-2025
It has been determined that certain Convenience kits that were packaged in breather pouch lot 323080002 may result in the potential of using non-sterile product if the vendor seal of the…
Class IIFDA: OngoingMEDLINE INDUSTRIES, LP - Northfield
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
September 2026363 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categoriesOctober 2025455 records · 4 categories